Andrey Ziyatdinov

Biochemistry, Genetics and Molecular BiologyEngineeringAgricultural and Biological Sciences

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “Multitrait GWAS to connect disease variants and biological mechanisms”.

Multitrait GWAS to connect disease variants and biological mechanisms

PLoS Genetics(2021)10.1371/journal.pgen.1009713

N/A

0.550DataRank · unranked

38 citations

Vincent Laville, Zachary R. McCaw, Zihuai He, Vincent Guillemot, Carla Lasry +12 more

Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma

Nature Communications(2020)10.1038/s41467-020-14594-5

N/A

0DataRank · unranked

46 citations

Yuan Lin, Roxana Daneshjou, Andrey Ziyatdinov, Guðmar Þorleifsson, Adam J. Rubin +17 more

Multitrait genetic-phenotype associations to connect disease variants and biological mechanisms

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.26.172999

N/A

0DataRank · unranked

6 citations

Vincent Laville, Zachary R. McCaw, Zihuai He, Vincent Guillemot, Carla Lasry +11 more

Estimating the effective sample size in association studies of quantitative traits

G3 Genes Genomes Genetics(2021)10.1093/g3journal/jkab057

N/A

0DataRank · unranked

27 citations

Jihye Kim, Dmitry Prokopenko, Florian Privé, Fabien Laporte, Po‐Ru Loh +3 more

Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies

BMC Medicine(2022)10.1186/s12916-022-02535-6

N/A

0DataRank · unranked

18 citations

Linda Kachuri, Rebecca E. Graff, Jovia L. Nierenberg, Khanh K. Thai, Stacey Alexeeff +90 more

Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.007

N/A

0DataRank · unranked

5 citations

Colleen Morse Kripke, Adam J. Mansfield, Alexander Li, Alexander Lopez, Alicia Hawes +95 more